食源性病原微生物核酸标准物质研制进展

doi:10.3969/j.issn.1000-1158.2023.03.20

Abstract
Figure/Table
References (53)
Related Citation (1)

Download: PDF (615 KB) HTML (1 KB)
Export: BibTeX | EndNote (RIS)

Abstract In order to ensure food safety, microbiological inspection for food hygiene must be attached importance. As the most commonly used microbial detection target, nucleic acid molecules require reference materials to realize traceability and provide a measurement basis. Nucleic acid reference materials are the sample standard to ensure the accuracy and consistency of nucleic acid test results. Here, the development of nucleic acid reference materials of several common foodborne pathogenic microorganisms were reviewed, in order to promote their application in food safety testing, and provide reference for improving the quality control level of microbial test results, ensuring the accuracy and impartiality of test results, and promoting the development of nucleic acid reference materials.

Key words： metrology foodborne bacteria foodborne virus nucleic acid reference materials microbial detection nucleic acid detection method food safety

Received: 27 July 2022 Published: 08 March 2023

PACS:

TB99

Fund:the National Natural Science Foundation of Chinaand the Agricultural Science and Technology Innovation Program of CAAS

	Service

	E-mail this article
	Add to my bookshelf
	Add to citation manager
	E-mail Alert
	RSS
	Articles by authors
	CHEN Tian-qi
	QI Xin
	WANG Min
	LI Kai
	FAN Li
	LI Liang

Cite this article:

CHEN Tian-qi,QI Xin,WANG Min, et al. Development Progress of Nucleic Acid Reference Materials for Foodborne Pathogenic Microorganisms[J]. Acta Metrologica Sinica, 2023, 44(3): 464-471.

URL:

http://jlxb.china-csm.org:81/Jwk_jlxb/EN/10.3969/j.issn.1000-1158.2023.03.20 OR http://jlxb.china-csm.org:81/Jwk_jlxb/EN/Y2023/V44/I3/464

	Wu Q P, Li Y D, Zhang J M. Advances in metabolomics of common food-borne pathogen［J］. Microbiology China, 2016, 43(3): 609-618.
［4］	Trapmann S, Catalani P, Hoorfar J, et al. Development of a novel approach for the production of dried genomic DNA for use as standards for qualitative PCR testing of food-borne pathogens［J］. Accreditation and Quality assurance, 2004, 9(11): 695-699.
［8］	李达,王军,杨忠,等.核酸标准物质定值的实验体系研究［J］.计量学报,2020,41(11):1436-1442.
［10］	林鹰,杨文莉,周玲艳,等.农业转基因核酸标准物质研究进展［J］.生物技术通报,2022,38(8):52-59.
［11］	牛春艳,张永卓,杨佳怡,等.基于数字PCR的质粒核酸标准物质合作定值研究［J］.计量学报,2021,42(11):1522-1527.
［13］	Zitz U, Zunabovic M, Domig K J, et al. Reduced detectability of Listeria monocytogenes in the presence of Listeria innocua［J］. Journal of Food Protection, 2011, 74(8): 1282-1287.
［16］	刘刚,李妍,许丽.一种特异性检测单增李斯特菌的质粒DNA标准物质［J］.化学试剂,2016,38(7):664-668.
［17］	JJG 1006—1994,一级标准物质技术规范［S］．
	Wu Q P, Kou X X, Zhang J M. Foodborne viruses and its detection methods［J］. Microbiology China, 2004(3): 101-105.
	Zhao J. Current situation of food safety in China and application of new detection technology［J］. China Food, 2019(Z1): 244-245.
［9］	赵雨佳,廖湉毅,范培蕾,等.核酸标准物质的研究进展［J］.计量科学与技术,2022,66(2):15-20.
	Tian J, Liu X M. Risk Assessment of Listeria monocytogenes in Foods［J］. Chinese Journl of Food Hygiene, 2009, 21(5): 468-472.
［20］	Goode B, OReilly C, Dunn J, et al. Outbreak of Escherichia coli O157: H7 Infections After Petting Zoo Visits, North Carolina State Fair, October-November 2004［J］. Archives of Pediatrics and Adolescent Medicine, 2009, 163(1): 42-48.
［22］	Verweyen H M, Karch H, Brandis M, et al. Enterohemorrhagic Escherichia coli infections: following transmission routes［J］. Pediatric Nephrology, 2000, 14(1): 73-83.
［24］	Iwaarden P V, Philipp W, Catalani P, et al. Certification of a Reference Material of Purified Genomic DNA from Escherichia Coli O157 (EDL 933) Certified Reference Material IRMM-449［R］. IRMM EU, EUR Report 22110, 2006.
［26］	Liang W, Xu L, Sui Z, et al. Quantification of plasmid DNA reference materials for Shiga toxin-producing Escherichia coli based on UV, HR-ICP-MS and digital PCR［J］. Chemistry Central Journal, 2016, 10(1): 1-10.
［30］	Guibourdenche M, Roggentin P, Mikoleit M, et al. Supplement 2003—2007 (No.47) to the White-Kauffmann-Le minor scheme ［J］. Res Microbiol, 2010, 161(1): 26-29.
［32］	Mezal E, Sabol A, Khan M, et al. Isolation and molecular characterization of Salmonella enterica serovar enteritidis from poultry house and clinical samples during 2010 ［J］. Food Microbiol, 2014, 38: 67-74.
［34］	Vallejo C V, Tere C P, Calderon M N, et al. Development of a genomic DNA reference material for Salmonella enteritidis detection using polymerase chain reaction［J］. Molecular and Cellular Probes, 2021, 55: 101690.
	Nusereti A, Yuan M Y, Lin X F, et al. Preparation of plasmid DNA reference material for Salmonella typhi［J］. Journal of Molecular Diagnostics and Therapy, 2020, 12(12): 1740-1744.
［1］	赵军.我国食品安全现状及检测新技术的应用［J］.中国食品,2019(Z1):244-245.
［5］	Rijpens N P, Herman L M F. Molecular methods for identification and detection of bacterial food pathogens［J］. Journal of AOAC International, 2002, 85(4): 984-995.
［6］	Mackay I M, Arden K E, Andreas N. Real-time PCR in virology［J］. Nucleic Acids Reseah, 2002,6:1292-305.
	Li D, Wang J, Yang Z, et al. Experimental design analysis of developing quantitative nucleic acid reference materials［J］. Acta Metrologica Sinica, 2020,41(11):1436-1442.
	Niu C Y, Zhang Y X, Yang J Y, et al. Research on the collaborative value assignment of plasmid nucleic acid refernce materials based on digital PCR［J］. Acta Metrologica Sinica, 2021, 42(11): 1522-1527.
［12］	罗超,李妍,赵珂珂,等.单核细胞增生李斯特氏菌标准物质冻干保存方法［J］.上海计量测试,2019,46(4):6-10.
［14］	田静,刘秀梅.食品中单核细胞增生李斯特氏菌的风险评估［J］.中国食品卫生杂志,2009,21(5):468-472.
［18］	蒲泽南,林晓峰,袁暮云,等.单核细胞增生李斯特菌质粒DNA参考物质的研制［J］.中国食品卫生杂志,2021,33(3):279-284.
［21］	Mohawk K L, OBrien A D. Mouse models of Escherichia coli O157: H7 infection and shiga toxin injection［J］. Journal of Biomedicine and Biotechnology, 2011(5):258185.
［36］	袁慕云,许龙岩,柯碧霞,等.实时荧光PCR技术在沙门菌种间鉴别中的应用［J］.中国卫生检验杂志,2017,27(16):2291-2294.
［39］	徐振波,刘晓晨,李琳,等.金黄色葡萄球菌肠毒素在食源性微生物中的研究进展［J］.现代食品科技,2013,29(9):2317-2324.
［7］	Kubista M, Andrade J M, Bengtsson M, et al. The real-time polymerase chain reaction［J］. Molecular aspects of medicine, 2006, 27(2-3): 95-125.
	Luo C, Li Y, Zhao k k, et al. Freeze-drying and preservation method studies on Standard Reference Materials of Listeria monocytogenes［J］. Shanghai Metrology and Testing, 2019, 46(4): 6-10.
	Pu Z N, Lin X F, Yuan M Y, et al. Preparation of plasmid DNA reference material for Listeria monocytogenes［J］. Chinese Journal of Food Hygiene, 2021, 33(3): 279-284.
［19］	Nguyen Y, Sperandio V. Enterohemorrhagic E. coli (EHEC) pathogenesis［J］. Frontiers in Cellular and Infection Microbiology, 2012, 2: 90.
［27］	World Health Organization. WHO estimates of the global burden of foodborne diseases: foodborne disease burden epidemiology reference group 2007-2015［M］. Geneva: WHO Press, 2015.
［28］	Xiong D, Song L, Pan Z M, et al. Identification and Discrimination of Salmonella enterica serovar gallinarum biovars pullorum and gallinarum based on a one-step multiplex PCR［J］． Frontiers in Microbiology, 2018, 9: 1718．
［29］	Yang Q, Wang F, Jones K L, et al. Evaluation of loop-mediated isothermal amplification for the rapid, reliable, and robust detection of Salmonella in produce［J］. Food Microbiology, 2015, 46: 485-493.
［31］	Wang Y, Yang B, Wu Y, et al. Molecular characterization of Salmonella enterica serovar enteritidis on retail raw poultry in six provinces and two national cities in China ［J］. Food Microbiol, 2015, 46: 74-80.
	Yuan M Y, Xu L Y, Ke B X, et al. Species differentiation and identification in Salmonella isolates by real-time PCR［J］. Chinese Journal of Health Laboratory Technology, 2017, 27(16): 2291-2294.
［37］	Chiefari A K, Perry M J, Kelly-Cirino C, et al. Detection of Staphylococcus aureus enterotoxin production genes from patient samples using an automated extraction platform and multiplex real-time PCR［J］. Molecular and cellular probes, 2015, 29(6): 461-467.
	Xu Z B, Liu X C, Li L, et al. Development of Staphylococcus aureus enterotoxin in food-borne bacteria［J］. Modern Food Science and Technology, 2013, 29(9): 2317-2324.
	Chen C, Liang L, Wang C E, et al. Development of national reference for Staphylococcus aureus nucleic acid detection kit［J］. Journal of Food Safety and Quality, 2021, 12(20): 8251-8257.
［52］	SN/T 2520—2010 贝类中A群轮状病毒检测方法.普通PCR和实时荧光PCR方法［S］.
［2］	吴清平,李玉冬,张菊梅.常见食源性致病菌代谢组学研究进展［J］. 微生物学通报, 2016, 43(3): 609-618.
［3］	JJF 1265—2010, 生物计量术语及定义［S］.
	Zhao Y J, Liao T Y, Fan P L, et al. A oerspective on nucleic acid reference materials［J］. Metrology Science and Technology, 2022, 66(2): 15-20.
	Lin Y, Yang W L, Zhou L Y, et al. Research Progress in Agricultural Genetically Modified Nucleic Acid Reference Materials［J］. Biotechnology Bulletin, 2022, 38(8): 52-59.
［15］	de Noordhout C M, Devleesschauwer B, Angulo F J, et al. The global burden of listeriosis: a systematic review and meta-analysis［J］. The Lancet Infectious Diseases, 2014, 14(11): 1073-1082.
	Liu G, Li Y, Xu L. Plasmid DNA Standard Ｒeference Material for the Specific Detection of Listeria Monocytogenes［J］. Chemical Reagents, 2016, 38(7): 664-668.
［23］	Phillips M M, Seal T M L, Ness J M, et al. Development and characterization of a Multimycotoxin reference material［J］. Journal of AOAC International, 2019, 102(6): 1642-1650.
［25］	Philipp W J, van Iwaarden P, Schimmel H, et al. Development of reference materials for microbiological analysis［J］. Accreditation and Quality Assurance, 2007, 12(3): 134-138.
［33］	Authority E F S, Prevention E C F D. The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2011［J］. EFSA Journal, 2013, 11(4): 3129.
［35］	努色热提·阿布都沙拉木,袁慕云,林晓峰,等.伤寒沙门氏菌质粒DNA参考物质的研制［J］.分子诊断与治疗杂志,2020,12(12):1740-1744.
［40］	陈驰,梁丽,王春娥,等.金黄色葡萄球菌核酸检测试剂盒用国家参考品的研制［J］.食品安全质量检测学报,2021,12(20):8251-8257.
［41］	吴清平,寇晓霞,张菊梅.食源性病毒及其检测方法［J］.微生物学通报,2004(3):101-105.
［42］	Farahmand M, Moghoofei M, Dorost A, et al. Global prevalence and genotype distribution of norovirus infection in children with gastroenteritis: A meta-analysis on 6 years of research from 2015 to 2020［J］. Reviews in Medical Virology, 2022, 32(1): e2237.
［43］	Sadiq A, Bostan N, Yinda K C, et al. Rotavirus: Genetics, pathogenesis and vaccine advances［J］. Reviews in Medical Virology, 2018, 28(6): e2003.
［44］	Vinjé J, Green J, Lewis D C, et al. Genetic polymorphism across regions of the three open reading frames of “Norwalk-like viruses” ［J］. Archives of Virology, 2000, 145(2): 223-241.
［48］	张奇,姚琳,江艳华,等.基于Qbeta噬菌体装甲RNA技术的诺如病毒RNA标准参考样品的研制［J］.中国生物工程杂志,2018,38(1):42-50.
［49］	王鸣秋,杨俊,常雨桐,等.GⅠ/GⅡ型诺如病毒两联装甲RNA标准样品的研制［J］.现代食品科技,2021,37(3):286-293,131.
［38］	Zeinhom M M A, Abdel-Latef G K, Jordan K. The use of multiplex PCR to determine the prevalence of enterotoxigenic Staphylococcus aureus isolated from raw milk, feta cheese, and hand swabs［J］. Journal of Food Science, 2015, 80(12): M2932-M2936.
［45］	Atmar R L, Opekun A R, Gilger M A, et al. Norwalk virus shedding after experimental human infection.［J］. Emerging Infectious Diseases, 2008, 14(10): 1553-1557.
［53］	徐蕾蕊,魏海燕,马丹,等.轮状病毒核酸标准物质研究［J］.中国食品学报,2018,18(7):201-209.
［46］	Pasloske B L, Walkerpeach C R, Obermoeller R D, et al. Armored RNA technology for production of ribonuclease-resistant viral RNA controls and standards［J］. Journal of Clinical Microbiology, 1998, 36(12): 3590-3594.
［47］	Song L, Sun S, Li B, et al. External Quality Assessment for Enterovirus 71 and Coxsackievirus A16 Detection by Reverse Transcription-PCR Using Armored RNA as a Virus Surrogate［J］. Journal of Clinical Microbiology, 2011, 49(10):3591-3595.
	Zhang Q, Yao L, Jiang Y H, et al. Development of armored RNA reference material of Norovirus based on Qbeta bacteriophage［J］. China Biotechnology, 2018, 38(1): 42-50.
	Wang M Q, Yang J, Chang Y T, et al. Preparation of coupled armored RNA reference material for Norovirus GI/GII［J］. Modern Food Science and Technology, 2021, 37(3): 286-293,131.
［51］	Tate J E, Burton A H, Boschi-Pinto C, et al. Global, regional, and national estimates of rotavirus mortality in children <5 years of age, 2000—2013［J］. Clinical Infectious Diseases, 2016, 62(suppl_2): S96-S105.
	Xu L R, Wei H Y, Ma D, et al. Establishment of a Nucleic Reference Material for Rotavirus Detection［J］. Journal of Chinese Institute of Food Science and Technology, 2018, 18(7): 201-209.
［50］	Roczo-Farkas S, Kirkwood C D, Bines J E. Australian rotavirus surveillance program: annual report, 2016［J］. Communicable Diseases Intelligence, 2017, 41(4): E455-E471.